# Clinical advances and challenges of anti-angiogenic targeted therapy in gastric cancer

**Authors:** Zhongyue Wu, Jiaojiao Ni, Qi Xu

PMC · DOI: 10.3389/fonc.2025.1654300 · Frontiers in Oncology · 2025-10-23

## TL;DR

This review explores how targeting blood vessel growth in gastric cancer can improve treatment, focusing on approved and emerging drugs and the need for better biomarkers.

## Contribution

The paper systematically evaluates clinical advancements and challenges in anti-angiogenic therapy for gastric cancer and highlights the role of biomarkers.

## Key findings

- Ramucirumab is the only approved anti-angiogenic drug for second-line gastric cancer therapy.
- Apatinib and fruquintinib show promise, especially when combined with immunotherapy.
- Predictive biomarkers remain limited, necessitating better patient stratification strategies.

## Abstract

Gastric cancer (GC) is a malignant neoplasm with one of the highest incidence and mortality rates. However, therapeutic options remain limited for advanced disease. Angiogenesis, a fundamental process in tumor progression, has emerged as a key therapeutic target. To comprehensively evaluate the clinical advancements of anti-angiogenic targeted drugs, this review conducted a systematic search and collation of pertinent literature, While, only ramucirumab achieved regulatory approval for second-line therapy, emerging agents including apatinib and fruquintinib demonstrate significant clinical benefits, particularly in combination with immunotherapy. The review also classifies and summarizes biomarkers with potential predictive value for treatment response, and discusses the current major challenges and potential optimization strategies. This analysis identifies significant gaps in predictive biomarkers and emphasizes that patient stratification and rational combination strategies are essential for optimizing therapeutic outcomes.

## Linked entities

- **Chemicals:** apatinib (PubChem CID 45139106), fruquintinib (PubChem CID 44480399)
- **Diseases:** gastric cancer (MONDO:0001056)

## Full-text entities

- **Diseases:** malignant neoplasm (MESH:D009369), GC (MESH:D013274)
- **Chemicals:** ramucirumab (MESH:C543333), fruquintinib (MESH:C000591844), apatinib (MESH:C553458)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12588871/full.md

## References

169 references — full list in the complete paper: https://tomesphere.com/paper/PMC12588871/full.md

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Source: https://tomesphere.com/paper/PMC12588871